AR078408A1 - DERIVATIVES OF INDOL AS MODULATORS OF THE CRAC - Google Patents
DERIVATIVES OF INDOL AS MODULATORS OF THE CRACInfo
- Publication number
- AR078408A1 AR078408A1 ARP100103446A ARP100103446A AR078408A1 AR 078408 A1 AR078408 A1 AR 078408A1 AR P100103446 A ARP100103446 A AR P100103446A AR P100103446 A ARP100103446 A AR P100103446A AR 078408 A1 AR078408 A1 AR 078408A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- alkoxy
- optionally substituted
- phenyl
- carbonyl
- Prior art date
Links
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical class C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 title 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 35
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 26
- 125000000217 alkyl group Chemical group 0.000 abstract 17
- 125000001072 heteroaryl group Chemical group 0.000 abstract 12
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 10
- 229910052736 halogen Inorganic materials 0.000 abstract 9
- 150000002367 halogens Chemical class 0.000 abstract 9
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 abstract 8
- 125000004356 hydroxy functional group Chemical group O* 0.000 abstract 7
- 150000002825 nitriles Chemical class 0.000 abstract 7
- 125000000623 heterocyclic group Chemical group 0.000 abstract 4
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 229910052739 hydrogen Inorganic materials 0.000 abstract 3
- 239000001257 hydrogen Substances 0.000 abstract 3
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- 125000004429 atom Chemical group 0.000 abstract 2
- 125000001424 substituent group Chemical group 0.000 abstract 2
- -1 -C1-6 alkyl nitrile Chemical class 0.000 abstract 1
- PSOPMMVKRIPMTJ-UHFFFAOYSA-N 1-(sulfonylmethyl)piperazine Chemical compound O=S(=O)=CN1CCNCC1 PSOPMMVKRIPMTJ-UHFFFAOYSA-N 0.000 abstract 1
- OTOIUCLFSQHFOX-UHFFFAOYSA-N 3-sulfonylmorpholine Chemical compound O=S(=O)=C1COCCN1 OTOIUCLFSQHFOX-UHFFFAOYSA-N 0.000 abstract 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 abstract 1
- 108090000312 Calcium Channels Proteins 0.000 abstract 1
- 102000003922 Calcium Channels Human genes 0.000 abstract 1
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 abstract 1
- 229910052791 calcium Inorganic materials 0.000 abstract 1
- 239000011575 calcium Substances 0.000 abstract 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/404—Indoles, e.g. pindolol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/08—Bronchodilators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
- C07D209/18—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Immunology (AREA)
- Pulmonology (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Transplantation (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Indole Compounds (AREA)
Abstract
Se describen también métodos de obtencion de los compuestos y el uso de los compuestos para el tratamiento de enfermedades asociadas con los canales de calcio activados con la liberacion de calcio (CRAC). Reivindicacion 1: Un compuesto de la formula (1): en la que: R1 es: - fenilo sustituido una, dos o tres veces por un grupo o grupo elegidos con independencia entre: alquilo C1-6; alcoxi C1-6; halogeno; halo-alquilo C1-6; halo-alcoxi C1-6; nitrilo; acetilo; (alcoxi C1-6)-carbonilo; aminocarbonilo; aminosulfonilo; (alquil C1-6)-carbonilamino; (alquil C1-6)-sulfanilo; (alquil C1-6)-sulfonilo; (alcoxi C1-6)-alquilo C1-6; hidroxi-alquilo C1-6; amino; hidroxi; sulfonilmorfolina; sulfonilmetilpiperazina; heterociclilo; fenilo que puede estar opcionalmente sustituido; o heteroarilo que puede estar opcionalmente sustituido; - piridinilo opcionalmente sustituido una o dos veces por un grupo o grupos elegidos con independencia entre: alquilo C1-6; alcoxi C1-6; halogeno; halo-alquilo C1-6 nitrilo; acetilo; (alcoxi C1-6)-carbonilo; (alquil C1-6)-carbonilamino; (alquil C1-6)-sulfanilo; (alquil C1-6)-sulfonilo; (alcoxi C1-6)-alquilo C1-6; hidroxi-alquilo C1-6; amino; oxo; hidroxi; heterociclilo; fenilo que puede estar opcionalmente sustituido; o heteroarilo que puede estar opcionalmente sustituido; - pirimidinilo opcionalmente sustituido una o dos veces por un grupo o grupos elegidos con independencia entre: alquilo C1-6; alcoxi C1-6; halogeno; halo-alquilo C1-6; nitrilo; acetilo; (alcoxi C1-6)-carbonilo; (alquil C1-6)-carbonilamino; (alquil C1-6)-sulfanilo; (alquil C1-6)-sulfonilo; (alcoxi C1-6)-alquilo C1-6; hidroxi-alquilo C1-6; amino; oxo; hidroxi; heterociclilo; fenilo que puede estar opcionalmente sustituido; o heteroarilo que puede estar opcionalmente sustituido; o - un anillo heteroarilo de cinco eslabones opcionalmente sustituido una, dos o tres veces por un grupo o grupos elegidos con independencia entre: alquilo C1-6; cicloalquilo C3-6; alcoxi C1-6; halogeno; halo-alquilo C1-6; nitrilo; acetilo; (alcoxi C1-6)-carbonilo; (alquil C1-6)-carbonilamino; (alquil C1-6)-sulfanilo; (alquil C1-6)-sulfonilo; (alcoxi C1-6)-alquilo C1-6; hidroxi-alquilo C1-6; amino; oxo; hidroxi; heterociclilo; fenilo que puede estar opcionalmente sustituido; y heteroarilo que puede estar opcionalmente sustituido; o dos de dichos sustituyentes junto con los átomos a los que están unidos pueden formar un fenilo fusionado con el anillo heteroarilo de cinco eslabones; es: - cicloalquilo C3-6; - fenilo sustituido una, dos o tres veces por un grupo o grupos elegidos con independencia entre: alquilo C1-6; alcoxi C1-6; alcoxihidroxi C1-6; halogeno; halo-alquilo C1-6; haloalcoxi C1-6; nitrilo; acetilo; (alcoxi C1-6)-carbonilo; (alquil C1-6)-carbonilamino; (alquil C1-6)-sulfanilo; (alquil C1-6)-sulfonilo; (alcoxi C1-6)-alquilo C1-6; hidroxi-alquilo C1-6; (alquil C1-6)-carbonilhidroxi; (alcoxi C1-6)-ciano; amino; hidroxi; fenilo que puede estar opcionalmente sustituido; o heteroarilo que puede estar opcionalmente sustituido; - piridinilo opcionalmente sustituido una o dos veces por un grupo o grupos elegidos con independencia entre: alquilo C1-6; alcoxi C1-6; halogeno; halo-alquilo C1-6; nitrilo; acetilo; (alcoxi C1-6)-carbonilo; (alquil C1-6)-carbonil- amino; (alquil C1-6)-sulfanilo; (alquil C1-6)-sulfonilo; (alcoxi C1-6)-alquilo C1-6; hidroxi-alquilo C1-6; amino; oxo; hidroxi; fenilo que puede estar opcionalmente sustituido; o heteroarilo que puede estar opcionalmente sustituido; - pirimidinilo opcionalmente sustituido una o dos veces por un grupo o grupos elegidos con independencia entre: alquilo C1-6; alcoxi C1-6; halogeno; halo-alquilo C1-6; nitrilo; acetilo; (alcoxi C1-6)-carbonilo; (alquil C1-6)-carbonilamino; (alquil C1-6)-sulfanilo; (alquil C1-6)-sulfonilo; (alcoxi C1-6)-alquilo C1-6; hidroxi-alquilo C1-6; fenilo que puede estar opcionalmente sustituido; o heteroarilo que puede estar opcionalmente sustituido; o - un anillo heteroarilo de cinco eslabones opcionalmente sustituido una o dos veces por un grupo o grupos elegidos con independencia entre: alquilo C1-6; alcoxi C1-6; halogeno; halo-alquilo C1-6; cicloalquilo C3-6; halo-alcoxi C1-6; nitrilo; acetilo; (alcoxi C1-6)-carbonilo; (alquil C1-6)-carbonilamino; (alquil C1-6)-sulfanilo; (alquil C1-6)-sulfonilo; (alcoxi C1-6)-alquilo C1-6; hidroxi-alquilo C1-6; amino; oxo; hidroxi; fenilo que puede estar opcionalmente sustituido; y heteroarilo que puede estar opcionalmente sustituido; o dos de dichos sustituyentes junto con los átomos a los que están unidos pueden formar un fenilo fusionado con dicho anillo heteroarilo de cinco eslabones; R3 es hidrogeno; R3' es hidrogeno o alquilo C1-6; es un numero de 0 a 3; cada R4 se elige con independencia entre: hidrogeno; alquilo C1-6; alcoxi C1-6; halogeno; y halo-alquilo C1-6, y dicha línea discontinua es un enlace o está ausente, o una sal farmacéuticamente aceptable de los mismos.Methods of obtaining the compounds and the use of the compounds for the treatment of diseases associated with calcium channels activated with calcium release (CRAC) are also described. Claim 1: A compound of the formula (1): wherein: R1 is: - phenyl substituted once, twice or three times by a group or group independently selected from: C1-6 alkyl; C1-6 alkoxy; halogen; halo C1-6 alkyl; C1-6 haloalkoxy; nitrile; acetyl; (C1-6 alkoxy) -carbonyl; aminocarbonyl; aminosulfonyl; (C1-6 alkyl) -carbonylamino; (C1-6 alkyl) -sulfanyl; (C1-6 alkyl) -sulfonyl; (C1-6 alkoxy) -C 1-6 alkyl; hydroxyC 1-6 alkyl; Not me; hydroxy; sulfonylmorpholine; sulfonylmethylpiperazine; heterocyclyl; phenyl that may be optionally substituted; or heteroaryl which may be optionally substituted; - pyridinyl optionally substituted once or twice by a group or groups chosen independently from: C1-6 alkyl; C1-6 alkoxy; halogen; halo-C1-6 alkyl nitrile; acetyl; (C1-6 alkoxy) -carbonyl; (C1-6 alkyl) -carbonylamino; (C1-6 alkyl) -sulfanyl; (C1-6 alkyl) -sulfonyl; (C1-6 alkoxy) -C 1-6 alkyl; hydroxyC 1-6 alkyl; Not me; oxo; hydroxy; heterocyclyl; phenyl that may be optionally substituted; or heteroaryl which may be optionally substituted; - pyrimidinyl optionally substituted once or twice by a group or groups chosen independently from: C1-6 alkyl; C1-6 alkoxy; halogen; halo C1-6 alkyl; nitrile; acetyl; (C1-6 alkoxy) -carbonyl; (C1-6 alkyl) -carbonylamino; (C1-6 alkyl) -sulfanyl; (C1-6 alkyl) -sulfonyl; (C1-6 alkoxy) -C 1-6 alkyl; hydroxyC 1-6 alkyl; Not me; oxo; hydroxy; heterocyclyl; phenyl that may be optionally substituted; or heteroaryl which may be optionally substituted; or - a five-link heteroaryl ring optionally substituted once, twice or three times by a group or groups chosen independently from: C1-6 alkyl; C3-6 cycloalkyl; C1-6 alkoxy; halogen; halo C1-6 alkyl; nitrile; acetyl; (C1-6 alkoxy) -carbonyl; (C1-6 alkyl) -carbonylamino; (C1-6 alkyl) -sulfanyl; (C1-6 alkyl) -sulfonyl; (C1-6 alkoxy) -C 1-6 alkyl; hydroxyC 1-6 alkyl; Not me; oxo; hydroxy; heterocyclyl; phenyl that may be optionally substituted; and heteroaryl which may be optionally substituted; or two of said substituents together with the atoms to which they are attached may form a phenyl fused with the five-link heteroaryl ring; is: - C3-6 cycloalkyl; - phenyl substituted once, twice or three times by a group or groups chosen independently from: C1-6 alkyl; C1-6 alkoxy; C1-6 alkoxyhydroxy; halogen; halo C1-6 alkyl; C1-6 haloalkoxy; nitrile; acetyl; (C1-6 alkoxy) -carbonyl; (C1-6 alkyl) -carbonylamino; (C1-6 alkyl) -sulfanyl; (C1-6 alkyl) -sulfonyl; (C1-6 alkoxy) -C 1-6 alkyl; hydroxyC 1-6 alkyl; (C1-6 alkyl) -carbonylhydroxy; (C1-6 alkoxy) -cyano; Not me; hydroxy; phenyl that may be optionally substituted; or heteroaryl which may be optionally substituted; - pyridinyl optionally substituted once or twice by a group or groups chosen independently from: C1-6 alkyl; C1-6 alkoxy; halogen; halo C1-6 alkyl; nitrile; acetyl; (C1-6 alkoxy) -carbonyl; (C1-6 alkyl) -carbonyl-amino; (C1-6 alkyl) -sulfanyl; (C1-6 alkyl) -sulfonyl; (C1-6 alkoxy) -C 1-6 alkyl; hydroxyC 1-6 alkyl; Not me; oxo; hydroxy; phenyl that may be optionally substituted; or heteroaryl which may be optionally substituted; - pyrimidinyl optionally substituted once or twice by a group or groups chosen independently from: C1-6 alkyl; C1-6 alkoxy; halogen; halo C1-6 alkyl; nitrile; acetyl; (C1-6 alkoxy) -carbonyl; (C1-6 alkyl) -carbonylamino; (C1-6 alkyl) -sulfanyl; (C1-6 alkyl) -sulfonyl; (C1-6 alkoxy) -C 1-6 alkyl; hydroxyC 1-6 alkyl; phenyl that may be optionally substituted; or heteroaryl which may be optionally substituted; or - a five-link heteroaryl ring optionally substituted once or twice by a group or groups independently selected from: C1-6 alkyl; C1-6 alkoxy; halogen; halo C1-6 alkyl; C3-6 cycloalkyl; C1-6 haloalkoxy; nitrile; acetyl; (C1-6 alkoxy) -carbonyl; (C1-6 alkyl) -carbonylamino; (C1-6 alkyl) -sulfanyl; (C1-6 alkyl) -sulfonyl; (C1-6 alkoxy) -C 1-6 alkyl; hydroxyC 1-6 alkyl; Not me; oxo; hydroxy; phenyl that may be optionally substituted; and heteroaryl which may be optionally substituted; or two of said substituents together with the atoms to which they are attached may form a phenyl fused with said five-link heteroaryl ring; R3 is hydrogen; R3 'is hydrogen or C1-6 alkyl; it is a number from 0 to 3; each R4 is independently selected from: hydrogen; C1-6 alkyl; C1-6 alkoxy; halogen; and haloC 1-6 alkyl, and said broken line is a bond or is absent, or a pharmaceutically acceptable salt thereof.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US24552109P | 2009-09-24 | 2009-09-24 | |
| US37806210P | 2010-08-30 | 2010-08-30 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR078408A1 true AR078408A1 (en) | 2011-11-02 |
Family
ID=43432437
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP100103446A AR078408A1 (en) | 2009-09-24 | 2010-09-22 | DERIVATIVES OF INDOL AS MODULATORS OF THE CRAC |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US20110071150A1 (en) |
| EP (1) | EP2480529A1 (en) |
| JP (2) | JP2013505913A (en) |
| KR (1) | KR20120068947A (en) |
| CN (1) | CN102574788A (en) |
| AR (1) | AR078408A1 (en) |
| BR (1) | BR112012006630A2 (en) |
| CA (1) | CA2771026A1 (en) |
| MX (1) | MX2012003539A (en) |
| RU (1) | RU2012116207A (en) |
| TW (1) | TW201121952A (en) |
| WO (1) | WO2011036130A1 (en) |
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| TWI423962B (en) * | 2009-10-07 | 2014-01-21 | Lg Life Sciences Ltd | Novel compounds effective as xanthine oxidase inhibitors, method for preparing the same, and pharmaceutical composition containing the same |
| JP2013530180A (en) | 2010-06-16 | 2013-07-25 | パーデュー、ファーマ、リミテッド、パートナーシップ | Aryl substituted indoles and uses thereof |
| US20130109720A1 (en) * | 2011-11-01 | 2013-05-02 | Hoffmann-La Roche Inc. | Indole inhibitors of crac |
| WO2013092444A1 (en) * | 2011-12-20 | 2013-06-27 | F. Hoffmann-La Roche Ag | Diazaindole inhibitors of crac |
| US20130158049A1 (en) * | 2011-12-20 | 2013-06-20 | Hoffmann-La Roche Inc. | 7-azaindole inhibitors of crac |
| US20130158066A1 (en) * | 2011-12-20 | 2013-06-20 | Hoffmann-La Roche Inc. | 4-azaindole inhibitors of crac |
| MX2015004500A (en) * | 2012-10-17 | 2015-07-06 | Hoffmann La Roche | 6-aminoindole derivatives as trp channel antagonists. |
| JP5758864B2 (en) | 2012-11-08 | 2015-08-05 | ファナック株式会社 | Brake drive control device for quickly changing the brake state from the released state to the engaged state |
| EP2738172A1 (en) | 2012-11-28 | 2014-06-04 | Almirall, S.A. | New bicyclic compounds as crac channel modulators |
| EP2970119B1 (en) * | 2013-03-14 | 2021-11-03 | Merck Sharp & Dohme Corp. | Novel indole derivatives useful as anti-diabetic agents |
| EP2848615A1 (en) | 2013-07-03 | 2015-03-18 | Almirall, S.A. | New pyrazole derivatives as CRAC channel modulators |
| EP3033342A1 (en) * | 2013-08-13 | 2016-06-22 | Grünenthal GmbH | Annelated pyrroles and their use as crac inhibitors |
| US9802920B2 (en) | 2013-12-13 | 2017-10-31 | Hoffman-La Roche Inc. | Inhibitors of bruton's tyrosine kinase |
| KR101824346B1 (en) | 2013-12-13 | 2018-01-31 | 에프. 호프만-라 로슈 아게 | Inhibitors of bruton's tyrosine kinase |
| CN106957252B (en) * | 2014-11-19 | 2019-11-19 | 连云港恒运药业有限公司 | A kind of proton pump inhibitor intermediate and preparation method thereof |
| MX378998B (en) | 2015-06-03 | 2025-03-11 | Bristol Myers Squibb Co | 4-HYDROXY-3-(HETEROARYL)PYRIDIN-2-ONE APELIN RECEPTOR AGONISTS (APJ) FOR USE IN THE TREATMENT OF CARDIOVASCULAR DISORDERS. |
| TW201835036A (en) | 2017-02-27 | 2018-10-01 | 瑞士商隆薩有限公司 | Method for preparation of 1-methyl-3-(trifluoromethyl)-1H-pyrazol-5-ol |
| WO2019018562A1 (en) | 2017-07-19 | 2019-01-24 | Ideaya Biosciences, Inc. | AMIDO COMPOUNDS AS AhR MODULATORS |
| WO2019099336A1 (en) | 2017-11-14 | 2019-05-23 | Bristol-Myers Squibb Company | Substituted indole compounds |
| JP7287964B2 (en) | 2017-12-15 | 2023-06-06 | ブリストル-マイヤーズ スクイブ カンパニー | substituted indole ether compounds |
| SG11202005696YA (en) | 2017-12-19 | 2020-07-29 | Bristol Myers Squibb Co | Substituted indole compounds useful as tlr inhibitors |
| EP3728253B1 (en) | 2017-12-19 | 2024-03-27 | Bristol-Myers Squibb Company | 6-azaindole compounds |
| SG11202005700SA (en) | 2017-12-19 | 2020-07-29 | Bristol Myers Squibb Co | Amide substituted indole compounds useful as tlr inhibitors |
| MX2020006014A (en) | 2017-12-20 | 2020-08-17 | Bristol Myers Squibb Co | Diazaindole compounds. |
| ES2965182T3 (en) * | 2017-12-20 | 2024-04-11 | Bristol Myers Squibb Co | Aryl and heteroaryl substituted indole compounds |
| SG11202005694RA (en) | 2017-12-20 | 2020-07-29 | Bristol Myers Squibb Co | Amino indole compounds useful as tlr inhibitors |
| BR112021004893A2 (en) | 2018-09-14 | 2021-06-01 | Rhizen Pharmaceuticals A G | compositions comprising a crac inhibitor and a corticosteroid and methods of using them |
| EP3628669A1 (en) * | 2018-09-28 | 2020-04-01 | GenKyoTex Suisse SA | Novel compounds as nadph oxidase inhibitors |
| CN112955450A (en) | 2018-10-24 | 2021-06-11 | 百时美施贵宝公司 | Substituted indole and indazole compounds |
| KR102911861B1 (en) | 2018-10-24 | 2026-01-12 | 브리스톨-마이어스 스큅 컴퍼니 | substituted indole dimer compounds |
| ES2987832T3 (en) | 2019-05-09 | 2024-11-18 | Bristol Myers Squibb Co | Substituted benzimidazolone compounds |
| US12448395B2 (en) | 2019-10-01 | 2025-10-21 | Bristol-Myers Squibb Company | Substituted bicyclic heteroaryl compounds |
| WO2021067657A1 (en) | 2019-10-04 | 2021-04-08 | Bristol-Myers Squibb Company | Substituted carbazole compounds |
| TW202227432A (en) | 2020-08-19 | 2022-07-16 | 美商必治妥美雅史谷比公司 | Substituted bicyclic compounds useful as inhibitors of tlr9 |
| CN115043770B (en) * | 2022-07-21 | 2023-09-08 | 南京大学 | Light-induced synthesis method of indole/azaindole compounds |
| CN115124410B (en) * | 2022-08-13 | 2024-06-04 | 上海珂华生物科技有限公司 | Preparation method of 2-fluoro-4-hydroxybenzaldehyde |
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| JPS5785055A (en) * | 1980-11-18 | 1982-05-27 | Konishiroku Photo Ind Co Ltd | Silver halide photographic recording material |
| JP2894617B2 (en) * | 1989-12-16 | 1999-05-24 | 帝国臓器製薬株式会社 | 2-phenylindole derivatives |
| FR2824827B1 (en) * | 2001-05-17 | 2004-02-13 | Fournier Lab Sa | NOVEL 5-PHENYL-1H-INDOLE ANTAGONIST DERIVATIVES OF INTERLEUKIN-8 RECEPTORS |
| WO2003099206A2 (en) * | 2002-05-21 | 2003-12-04 | Bristol-Myers Squibb Company | Indole compounds useful as impdh inhibitors |
| GB0602768D0 (en) * | 2006-02-10 | 2006-03-22 | Vastox Plc | Treatment of muscular dystrophy |
| KR101472248B1 (en) * | 2006-02-10 | 2014-12-16 | 서미트 코포레이션 피엘씨 | Treatment of duchenne muscular dystrophy |
| US20090142832A1 (en) * | 2007-11-29 | 2009-06-04 | James Dalton | Indoles, Derivatives, and Analogs Thereof and Uses Therefor |
| WO2010045188A1 (en) * | 2008-10-17 | 2010-04-22 | Boehringer Ingelheim International Gmbh | Heteroaryl substituted indole compounds useful as mmp-13 inhibitors |
| WO2010093191A2 (en) * | 2009-02-13 | 2010-08-19 | Lg Life Sciences Ltd. | Novel compounds effective as xanthine oxidase inhibitors, method for preparing the same, and pharmaceutical composition containing the same |
| NZ595410A (en) * | 2009-03-27 | 2013-12-20 | Merck Sharp & Dohme | Inhibitors of hepatitis c virus replication |
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2010
- 2010-09-21 CA CA2771026A patent/CA2771026A1/en not_active Abandoned
- 2010-09-21 KR KR1020127010486A patent/KR20120068947A/en not_active Ceased
- 2010-09-21 WO PCT/EP2010/063838 patent/WO2011036130A1/en not_active Ceased
- 2010-09-21 CN CN2010800426038A patent/CN102574788A/en active Pending
- 2010-09-21 EP EP10754941A patent/EP2480529A1/en not_active Withdrawn
- 2010-09-21 RU RU2012116207/04A patent/RU2012116207A/en not_active Application Discontinuation
- 2010-09-21 JP JP2012530236A patent/JP2013505913A/en active Pending
- 2010-09-21 MX MX2012003539A patent/MX2012003539A/en not_active Application Discontinuation
- 2010-09-21 BR BR112012006630A patent/BR112012006630A2/en not_active Application Discontinuation
- 2010-09-22 AR ARP100103446A patent/AR078408A1/en unknown
- 2010-09-23 TW TW099132213A patent/TW201121952A/en unknown
- 2010-09-23 US US12/888,701 patent/US20110071150A1/en not_active Abandoned
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2012
- 2012-08-15 JP JP2012180132A patent/JP2012246302A/en active Pending
Also Published As
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|---|---|
| KR20120068947A (en) | 2012-06-27 |
| JP2013505913A (en) | 2013-02-21 |
| CA2771026A1 (en) | 2011-03-31 |
| RU2012116207A (en) | 2013-10-27 |
| MX2012003539A (en) | 2012-04-30 |
| TW201121952A (en) | 2011-07-01 |
| WO2011036130A1 (en) | 2011-03-31 |
| JP2012246302A (en) | 2012-12-13 |
| US20110071150A1 (en) | 2011-03-24 |
| CN102574788A (en) | 2012-07-11 |
| BR112012006630A2 (en) | 2016-05-03 |
| EP2480529A1 (en) | 2012-08-01 |
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